JPS5847064A - Epoxy resin powder paint composition - Google Patents

Epoxy resin powder paint composition

Info

Publication number
JPS5847064A
JPS5847064A JP14537781A JP14537781A JPS5847064A JP S5847064 A JPS5847064 A JP S5847064A JP 14537781 A JP14537781 A JP 14537781A JP 14537781 A JP14537781 A JP 14537781A JP S5847064 A JPS5847064 A JP S5847064A
Authority
JP
Japan
Prior art keywords
epoxy resin
resistance
curing
powder paint
coating film
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP14537781A
Other languages
Japanese (ja)
Inventor
Minoru Hosoda
細田 実
Masahiko Kubo
正彦 久保
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Dai Nippon Toryo KK
Original Assignee
Dai Nippon Toryo KK
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Dai Nippon Toryo KK filed Critical Dai Nippon Toryo KK
Priority to JP14537781A priority Critical patent/JPS5847064A/en
Publication of JPS5847064A publication Critical patent/JPS5847064A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To provide a quick-curing powder paint compsn. consisting of powdery epoxy resin particles and glass flakes and forming a coating film excellent in flexing resistance, impact resistance at low temperature and cathode peel resistance. CONSTITUTION:The paint compsn. in made from powdery epoxy resin particles (A) consisting of a bisphenol type epoxy resin (e.g., an epoxy resin obtained by condensation of bisphenol A with epichlorohydrin and having an epoxy equivalent of about 700-5,000 and a melting point of about 90-155 deg.C), hardener (e.q., phthalic anhydride, dicyandiamide, adipic hydrazide, 2-methylimidazoline or 2- methylimidazole) and pigment, and glass flakes (B) with an average thickness of 0.5-10mu and an average size of 20-500mu which are used in 5-20wt% of (A). The coating film is in no way inferior to that of conventional powder paint in flexing resistance, shows excellent low temperature impact resistance and cathode peel resistance, and is quick-curing.

Description

【発明の詳細な説明】 に関する。[Detailed description of the invention] Regarding.

従来、鉄筋や鋼管等のよ5な熱谷振の非電に大きな被塗
物に対する粉体塗装は、被塗物を220〜〜.2IIO
℃に予熱し、静電スデレー等により塗装しよる再塗装が
できないため、塗膜による保mを確実にするに%工=度
でコsoーtIooμ程度の厚膜に塗装すること、加え
て予熱のみで浴融、速硬化するタイプの粉体塗料を塗布
することが必要であった。
Conventionally, powder coating of large non-electrical objects such as reinforcing bars and steel pipes, etc., has been carried out at a temperature of 220~. 2IIO
Since repainting cannot be done by preheating to ℃ and painting with electrostatic spray, etc., in order to ensure that the paint film retains its thickness, it is necessary to apply a thick film of about 100μ in % work = degree, and in addition, preheat. It was necessary to apply a type of powder coating that melts in a bath and hardens quickly.

通常このようなタイプの粉体塗料を用いた塗装方法はF
usion Bonded Coating(F日C)
と呼ばれている。
The coating method using this type of powder coating is usually F.
Usion Bonded Coating (F day C)
It is called.

近年、大型のパイプラインデロジエクトカ次々に生れ、
又それらの敷設場所がアラスカ、シペリャ等の寒冷地に
及ぶに至って、従来の外向核種に使用されて(・2/リ
エチレン・ライニングの欠点を改曳するものとしてFB
C柑の速硬化型エポ牟シ樹脂粉体塗料が注目されて米友
In recent years, large pipeline construction vehicles have been born one after another,
In addition, as they have been installed in cold regions such as Alaska and Sipella, they have been used for conventional extroverted nuclides (2/FB as a solution to overcome the drawbacks of polyethylene lining.
C-Kan's fast-curing epoxy resin powder paint attracted attention and won Yoneyu.

この種の塗料は速硬化性が要求されるのは勿論のこと、
苛酷な使用条件に耐えるため、その塗膜性能は耐低温屈
曲性、耐低温衝撃性、耐熱水浸慣性、耐陰極剥離性(防
食性)等において極めて高水準であることが要求されて
いる。
Of course, this type of paint requires fast curing,
In order to withstand harsh usage conditions, the coating film performance is required to be extremely high in terms of low-temperature flexibility, low-temperature impact resistance, hot water immersion resistance, cathodic peeling resistance (corrosion resistance), etc.

又、被塗物力1五パイプ等の長尺物である場合には、被
l11i物の自重による撓みが生じるため、それに付随
して塗膜の屈曲性も当然要求されている。
In addition, when the object to be coated is a long object such as a 15-meter pipe, the object to be coated is deflected due to its own weight, and accordingly, flexibility of the coating film is naturally required as well.

従って、上記の粉体塗料に於いては汎用のエポキン樹脂
粉体鹸科に比べて、rルタイムを短輔するために硬化促
進剤を添加したり、あるいは賛求される化学的、am埋
的性能を満足させるために、顔料の配曾濃iを変化させ
たりする試みがなされている。例えば、フェノール系の
硬化促進剤を用いたり、硬化剤として無水トリメリット
酸を併用したり、あるいはシリカ系顔料の菫を調節した
りすること等が行なわれている。
Therefore, in the above-mentioned powder coatings, compared to the general-purpose Epoquine resin powder coatings, curing accelerators are added in order to shorten the time required, or chemical or ammonium chloride treatment is recommended. In order to satisfy the performance, attempts have been made to change the pigment concentration i. For example, phenolic curing accelerators have been used, trimellitic anhydride has been used as a curing agent, or the violet color of silica pigments has been adjusted.

しかしながら、現状では耐低温衝撃性、耐陰極剥離性、
耐屈曲性等の全ての性能を十分満足する塗膜は得られて
いない。
However, at present, low-temperature impact resistance, cathodic peeling resistance,
A coating film that fully satisfies all properties such as bending resistance has not been obtained.

本発明は前述の如き現状に鑑みてなされたものであり、
塗膜の耐屈曲性等の性能は従来のものに比して優るとも
劣らず、しかも耐低温衝撃性及び耐陰極剥離性の非常に
優れた速硬化型エポキシ樹脂粉体塗料組成物を提供する
ことを目的とする@即ち、本発明は、 (A)  ビスフェノール型エポキシ樹脂と硬化剤及び
調料からなる粉末状エポキシ樹脂粒子と、但) 前記粉
末状エポキシ樹脂に対してS−コθ電1暢の、平均厚さ
0.S〜10μ、平均大きさ一〇〜SOOμのカラスフ
レーク、 とから成る速硬化型エポキシ樹脂粉体塗料組成物に係る
The present invention was made in view of the above-mentioned current situation,
To provide a fast-curing epoxy resin powder coating composition which has properties such as bending resistance of the coating film that are as good as those of conventional coatings, and which also has extremely excellent low-temperature impact resistance and cathodic peeling resistance. That is, the present invention has the following objects: (A) Powdered epoxy resin particles consisting of a bisphenol type epoxy resin, a curing agent, and a preparation; , average thickness 0. crow flakes having an average size of S~10μ and an average size of 10~SOOμ.

本発明に使用されるエポキシ樹脂は、ビスフェノールA
とエピクロルヒドリンの給付によって得られる、工Iキ
ン当蓋が約700−3000程度で融点2>1約9(1
)〜/45″clIjA&のビスフェノール型工Iキン
樹脂である。
The epoxy resin used in the present invention is bisphenol A
and epichlorohydrin, the yield is about 700-3000 and the melting point is 2>1 about 9 (1
)~/45″clIjA& bisphenol type resin.

上記エポキシ樹脂としては、シェル化学社製商品名エビ
オートioo亭 、f”J 1007 、チパ社裂商品
名アラルダイト60gダ、同6θ9り、同1.Q99.
閤709り、ダウ社製商品名DER66+、同667、
同bbg@の市販品等が使用し得る。
Examples of the epoxy resins include Shell Chemical Co., Ltd.'s trade name Ebiot Ioo-tei, f"J 1007, Chipa Co., Ltd.'s trade name Araldite 60g, 6θ9, and 1.Q99.
閤709ri, manufactured by Dow Company, product name DER66+, DER667,
Commercially available products such as bbg@ may be used.

又、前記硬化剤としては、無水フタル酸、無水トリメリ
ット酸等の酸無水物;シフアンジアミド;アジビン酸ジ
ヒドラジド等のジヒト°ラジド;コーメテルイミダゾリ
ン、−一フェニルイミタ゛ゾIJン等のイミダシリン;
コーメチルイミタ゛ゾール、コーエチルーダニメテルイ
ミダゾール、−一フェニルイミダ!−ル等の常温で固形
の硬化剤カニ便用し得る。これらは単独で、又1コ櫨以
上の混付物として使用し得る。
Further, as the curing agent, acid anhydrides such as phthalic anhydride and trimellitic anhydride; dihydrazide such as dihydrazide dihydrazide; imidacillin such as cometely imidazoline and -1 phenyl imidazoline;
Co-methyl imidazole, co-methyl imidazole, -phenylimida! - Can be used as a hardening agent that is solid at room temperature, such as in a mold. These can be used alone or in admixture with one or more oaks.

前記エポキシ樹脂と硬化剤&工、工4キシ樹月旨中のエ
ポキ7基と硬化剤中の活性水素カニ当量比前後になるよ
うな割付で混合され、さらに着色、防錆、塗膜物性改良
の目的で顔料(着色顔料、体1M顔料等)や、塗膜の流
動性を改良する目的で流動助卸]等の添加剤があらかじ
め混合され硬イヒ温度以下で溶融混合、粉砕後分級され
て平均粒子径20〜gθμ根度の本発明に使用する粉末
状工Iキン衛11旨粒子が得られる。
The above-mentioned epoxy resin and curing agent are mixed with the 7 epoxy groups in the hardening agent and the active hydrogen crab equivalent ratio in the curing agent, and are further colored, rust-prevented, and improve the physical properties of the coating film. Additives such as pigments (coloring pigments, 1M pigments, etc.) and fluid additives to improve the fluidity of the paint film are mixed in advance, melted and mixed at below the hardening temperature, and then crushed and classified. Powdered particles used in the present invention having an average particle diameter of 20 to gθμ are obtained.

前記着色顔料及び体質顔料等Q)IO4料bv、分&工
、ビスフェノール型エポキシ情(脂と硬化4jσ〕合計
量65〜SO重量部に対して20〜33 重量部便用す
ることが好ましい・ 更に、本発明においては平均厚さ0.5〜10μ、平均
大苧さ2O−QOpのカラスフレークを用いることが必
須要件である。該ガラスフレークは、前記ビスフェノー
ル型エポキンm脂、硬化剤、調料、必賛により其の他県
加削から成る粉末状エポキシ樹脂に対して5−.20電
瀘優のll1l甘で使用される。
The above-mentioned coloring pigments and extender pigments, etc.Q) IO4 materials bv, min & process, bisphenol type epoxy conditions (fat and curing 4jσ) It is preferable to use 20 to 33 parts by weight based on the total amount of 65 to 65 parts by weight of SO. In the present invention, it is essential to use glass flakes with an average thickness of 0.5 to 10 μm and an average diameter of 2O-QOp. It is also used at a rate of 5-.20 electric power for powdered epoxy resin made from other prefecture machining.

前記範囲において、ガラスフレークの混付童がS亀を鳴
に満たない場合は低温域(−5θ〜−60℃)における
耐衝単性や耐陰極剥離性を改良することが出来ず、逆に
コO重!憾をこえて使用さ扛ると低温域での屈曲性が低
下するためいずれも好ましくない。
In the above range, if the amount of mixed glass flakes is less than the S turtle, it will not be possible to improve the impact resistance and cathode peeling resistance in the low temperature range (-5θ to -60°C), and on the contrary, Koo heavy! Both are unfavorable because if they are used excessively, the flexibility in the low temperature range will decrease.

本発明のエポキシ樹脂粉体塗料組成物は、萌紀粉末状エ
ボキン樹脂とカラスフレークを均實になるまでトライブ
レンドすることによ!ll得られる。
The epoxy resin powder coating composition of the present invention is produced by tri-blending Moeki's powdered Evokin resin and crow flakes until they become homogeneous! Ill get it.

かくして得られた本発明の組成物は、2.20〜2’l
O℃h度に予熱された鋼管、鈎鉄管等の外(3)に静電
スプレー塗装により膜厚230−、−ダOOμ程厩に塗
装され、鋼管等の残熱により、5分以内に溶融、硬化し
成膜する。但し、被虻物の竪状、大きさ等により冷却速
匿が速い場合があるので必要に応じて後加熱してもよい
The composition of the present invention thus obtained has a volume of 2.20 to 2'l
The outside of steel pipes, hook iron pipes, etc. that have been preheated to 0℃h degrees (3) is electrostatically sprayed to a film thickness of about 230-, -00μ, and melts within 5 minutes due to the residual heat of the steel pipes, etc. , cure and form a film. However, since the cooling speed may be fast depending on the vertical shape, size, etc. of the target, post-heating may be performed if necessary.

本発明の組成物においては、飢荀後粉木状工4キ7樹脂
粒子が溶融流動する時に、カラスフレークは溶融偏平化
する樹脂粒子面に付層して移動し、かつ移動距離が最も
大きい位置にあることなどに伴ない、塗膜内に均一に、
かつ被堅物に平行に並ぶ割合が極めて太きいため、得ら
れた被膜の耐衝撃性や耐陰極刺離性が著しく向上Tるも
のと考えられる。
In the composition of the present invention, when the resin particles melt and flow after starvation, the crow flakes move as a layer on the surface of the resin particles that are melted and flattened, and the moving distance is the largest. Due to its location, it is uniformly distributed within the coating film.
In addition, since the proportion of the particles lining parallel to the object is extremely large, it is thought that the impact resistance and cathodic puncture resistance of the resulting coating are significantly improved.

かくして本発明の組成物は、パ“イプラ1ンあるいは埋
設鋼管等の外面塗装用粉体塗料組成物として工業的に極
めて有用である。
Thus, the composition of the present invention is industrially extremely useful as a powder coating composition for coating the exterior surfaces of pipelines, buried steel pipes, and the like.

以下本発明の好調を実施例により説明TるO「部」又ハ
「僑」は「重1[J又hs[本1ltjJをもって来丁
The success of the present invention will be explained below with examples.

実施例1 エポキン当@ qoo−toooのビスフェノール型工
Iキシ樹阪Sg部、無水トリメリット酸9.3部、質性
ジシアンジアミド〔ンエル化学表商品名Epikure
 OX −/ダダ〕コ、ys%w化チタン/コ部、タル
71g部をエクストルーダー中で加熱溶融、混線後、粉
砕、分級して平均粒子%30μの粉末状エポキシ樹脂粒
子を得几。
Example 1 Epoquin @ qoo-tooo's bisphenol-type compound I Kishijusaka Sg part, trimellitic anhydride 9.3 parts, dicyandiamide [Nel Chemical Table product name Epikure]
71 g of titanium oxide, ys% w titanium, and tal are melted in an extruder, mixed, crushed, and classified to obtain powdered epoxy resin particles with an average particle size of 30 μm.

ついで該粉末状エポキシfA脂粒子に、平均厚さ2〜S
μ、平均大きさIIooμのカラスフレークlOsを振
動混合し、本発明のエポキシ樹脂粉体塗料組成物を得た
Next, the powdered epoxy fA fat particles are coated with an average thickness of 2 to S.
The epoxy resin powder coating composition of the present invention was obtained by vibration-mixing crow flakes lOs having an average size of IIooμ.

得られた組Yft物をコ30℃に予熱されたコ0θ×1
0OX//■のグリッドプラスト鋼板上に静電スプレー
塗装により乾燥膜厚30θ〜330μになるよう塗布後
、230℃で後加熱を3分間行(・、比較試―に供した
The obtained set Yft was preheated to 30°C.
After coating on a 0OX//■ Grid Plast steel plate by electrostatic spray coating to a dry film thickness of 30θ to 330μ, post-heating was performed at 230°C for 3 minutes (a comparative test was performed).

実施例二〜ダ 第1表に示した配弁にエリ、前記実施例1と1司様にし
て本発明の工Iキ7樹脂粉体塗料組成物を得た後、同様
にして供試片を得、比較試験に供した。
Examples 2 to 2 The resin powder coating composition of the present invention was prepared using the valves shown in Table 1 in the same manner as in Example 1, and then test pieces were prepared in the same manner. was obtained and subjected to a comparative test.

M/表 実施例ユ〜qの配合 (単位二部) 1実施例ユ爽施例31実施伺ダ 1 タルク          − ’  tg  :
tg  ltg比較例1〜3 第2表に示した配合により、前6己爽施例1と同様にし
て比較例のエポキシ樹脂粉体槃科組成物を得た後、同様
にして供試片を得、比較試験に供した。
M/Table Formulation of Examples U to Q (Unit: 2 parts) 1 Example 31 Example 1 Talc -' tg:
tg ltg Comparative Examples 1 to 3 After obtaining epoxy resin powder perginate compositions of comparative examples in the same manner as in Example 1, using the formulations shown in Table 2, test pieces were prepared in the same manner. The sample was obtained and subjected to a comparative test.

第2衆  比較例配合 (単位二部) 第3表 比較試験結果表 (注/ )  ASTM(American 5oci
ety for TestingMaterials 
) G−/’Iに準拠し、S/gインチ怪の半球軟鉄の
先端部を撃芯とし、それを粉体m科塗膜に静置し、その
上から 2.3〜の鉄塊を路下させ、4膜に衝撃跡がつく衝撃エ
ネルギー値(インナーボンド)を求めた。
2nd batch Comparative example formulation (unit 2 parts) Table 3 Comparative test result table (note/ ) ASTM (American 5oci
ety for Testing Materials
) Based on G-/'I, use the tip of a hemispherical soft iron of S/g inch as a striking core, place it on a powder coating film, and then apply a 2.3 ~ iron ingot from above. The impact energy value (inner bond) at which impact marks were left on the four membranes was determined by letting it go down the road.

試験温服は−so℃にて実施。The test was carried out at -so°C.

(注2)  600X−〇 X 3.2−の帯状試験片
をiσ配実施例1と同様に塗布後、/、 j’のベンド
アングルV(相当するパイプに沿って曲げ、ワレ、ハガ
レ等の塗膜異常を確認した。
(Note 2) After applying a strip test piece of 600X-〇 An abnormality in the paint film was confirmed.

試験湿層しエーSθ℃にて実施。The test was carried out at Sθ℃ with a wet layer.

(注、?)  ASTM  G−gに準拠し、試験Hの
粉体塗膜面にドリルで径S■の穴をあけて鉄素地を露出
させる。試験片襄囲及び側面はタールエぞキン系塗料で
ンールし、さらにその上からパラフィンを塗布し完全に
絶縁状態とする。この試ぶ片を3優塩化ナトリウム水溶
液中に浸漬し、対極にカーボンを使い−/!00mVに
て30日間(常温)通電させる。
(Note, ?) In accordance with ASTM G-g, a hole with a diameter S■ is drilled on the powder coating surface of Test H to expose the iron base. The surroundings and sides of the test piece are coated with tar-ezokin-based paint, and then paraffin is applied over it to completely insulate it. This test piece was immersed in an aqueous sodium chloride solution, and carbon was used as the counter electrode. Electricity is applied at 00 mV for 30 days (at room temperature).

通電後試験片をとり出し、前記径5mの穴からカッター
ナイフで塗膜をはがし、最早はがれなくなった所でやめ
てその直径をfA11冗し九〇 前記比軟試験結果表より明かに、本発明の工lキン樹脂
粉体塗料組成物から得られ′fc、塗膜は、ガラスフレ
ーク無隋加(比較$11/)、カラスフレーク25畳添
加(比較例コ)及び鱗片状酸化鉄添加(比較例3)等に
比してjt低温衝撃性及び耐陰極剥離性において著しく
優れた結果を不した。
After energizing, take out the test piece and use a cutter knife to peel off the coating from the 5 m diameter hole, stop at the point where it no longer peels off, and measure the diameter. The coating film was obtained from a resin powder coating composition with no addition of glass flakes (comparison $11/), addition of 25 tatami of crow flakes (comparative example), and addition of scaly iron oxide (comparative example). 3), etc., the results were significantly superior in jt low-temperature impact resistance and cathode peeling resistance.

Claims (1)

【特許請求の範囲】[Claims] (1)囚 とスフエノール型工Iキン樹脂と、硬化剤及
び顔料1り成る粉末状エポキン樹脂粒子と、(B)  
前記粉末状エポキン樹脂に対してS−コO重量僑の、平
均厚さO0S〜10μ、平均大きさコO〜SOOμのカ
ラスフレーク、 とから成る速硬化型エポキシ樹脂粉体塗料組成物。 (A 前記硬化剤は、酸無水物、ンシアンジアミド、ジ
ヒドラジド、イミダシリンおよびイミダゾールから選ば
れたl樵もしくはコ柚以上の混合物である特許請求の範
囲第(1)項記載の速硬化型ニーキシ樹脂粉体塗料組成
物。
(1) Powdered Epoquine resin particles consisting of a powder, a suphenolic resin, a curing agent, and a pigment; (B)
A fast-curing epoxy resin powder coating composition comprising crow flakes having an average thickness of 0S to 10μ and an average size of 0 to SOOμ, the weight of which is smaller than the powdered epoxy resin. (A) The fast-curing nixy resin according to claim (1), wherein the curing agent is a mixture of at least one or more selected from acid anhydride, cyandiamide, dihydrazide, imidacillin, and imidazole. Powder coating composition.
JP14537781A 1981-09-14 1981-09-14 Epoxy resin powder paint composition Pending JPS5847064A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP14537781A JPS5847064A (en) 1981-09-14 1981-09-14 Epoxy resin powder paint composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14537781A JPS5847064A (en) 1981-09-14 1981-09-14 Epoxy resin powder paint composition

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JPS5847064A true JPS5847064A (en) 1983-03-18

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JP14537781A Pending JPS5847064A (en) 1981-09-14 1981-09-14 Epoxy resin powder paint composition

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63193284A (en) * 1987-02-06 1988-08-10 Nippon Sheet Glass Co Ltd Vector discriminating device
JPH02101586A (en) * 1988-10-11 1990-04-13 Agency Of Ind Science & Technol Adaptive learning type general purpose picture measuring system
JPH02101591A (en) * 1988-10-11 1990-04-13 Agency Of Ind Science & Technol Adaptive learning type general purpose picture measuring device
US20120258316A1 (en) * 2009-07-29 2012-10-11 Akzo Nobel Coatings International B.V. Powder coating compositions capable of having a substantially non-zinc containing primer

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63193284A (en) * 1987-02-06 1988-08-10 Nippon Sheet Glass Co Ltd Vector discriminating device
JPH02101586A (en) * 1988-10-11 1990-04-13 Agency Of Ind Science & Technol Adaptive learning type general purpose picture measuring system
JPH02101591A (en) * 1988-10-11 1990-04-13 Agency Of Ind Science & Technol Adaptive learning type general purpose picture measuring device
US20120258316A1 (en) * 2009-07-29 2012-10-11 Akzo Nobel Coatings International B.V. Powder coating compositions capable of having a substantially non-zinc containing primer
US10011736B2 (en) * 2009-07-29 2018-07-03 Akzo Nobel Coatings International B.V. Powder coating compositions capable of having a substantially non-zinc containing primer
US20180282572A1 (en) * 2009-07-29 2018-10-04 Akzo Nobel Coatings International B.V. Powder Coating Compositions Capable of Having a Substantially Non-Zinc Containing Primer
US10550283B2 (en) 2009-07-29 2020-02-04 Akzo Nobel Coating International B.V. Powder coating compositions capable of having a substantially non-zinc containing primer

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